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全磁悬浮左心室辅助装置的左心室尺寸与临床结局

Left Ventricular Dimensions and Clinical Outcomes With a Fully Magnetically Levitated Left Ventricular Assist Device.

作者信息

Molina Ezequiel J, Ahmed Mustafa M, Sheikh Farooq H, Cleveland Joseph C, Goldstein Daniel J, Uriel Nir Y, Wang AiJia, Revis Jordan J, Mehra Mandeep R

机构信息

Piedmont Heart Institute, Atlanta, Georgia, USA.

University of Florida, Gainesville, Florida, USA.

出版信息

JACC Heart Fail. 2025 May;13(5):798-811. doi: 10.1016/j.jchf.2024.09.019. Epub 2024 Dec 18.

Abstract

BACKGROUND

Prior analyses have suggested that a smaller left ventricular end-diastolic diameter (LVEDD) is associated with reduced survival following HeartMate 3 left ventricular assist device implantation.

OBJECTIVES

In this trial-based comprehensive analysis, the authors sought to examine clinical characteristics and association with the outcome of this specific relationship.

METHODS

The authors analyzed the presence of LVEDD <55 mm among 1,921 analyzable HeartMate 3 patients within the MOMENTUM 3 (Multicenter Study of MagLev Technology in Patients Undergoing Mechanical Circulatory Support Therapy With HeartMate 3) trial portfolio, on endpoints of overall survival and adverse events at 2 years. Adverse events included hemocompatibility-related (stroke, bleeding, and pump thrombosis) and non-hemocompatibility-related (right heart failure, infection) outcomes.

RESULTS

Those with a smaller LVEDD (<55 mm) (n = 108) were older (age 63 ± 11 years vs 60 ± 12 years; P = 0.005), were more often female (31% vs 20%; P = 0.096), and had more ischemic cardiomyopathy (60.2% vs 42.6%; P = 0.0004) compared with the LVEDD ≥55 mm group (n = 1,813). Death during implant hospitalization was higher (14.8 vs 5.7%; P = 0.0007) and survival at 2 years was lower (63.3% vs 81.8%; HR: 1.97 [95% CI: 1.39-2.79]; P = 0.0002) in the LVEDD <55 mm group. The LVEDD <55 mm group experienced more deaths due to hemocompatibility-related adverse events (2.8% vs 0.6%; HR: 4.61 [95% CI: 1.29-16.45]; P = 0.018) and right heart failure, both early (0-30 days; 7.4% vs 2.0%; HR: 3.70 [95% CI: 1.73-7.91]; P = 0.001) and late (>30 days; 12.0 vs 4.8%; HR: 2.58 [95% CI: 1.37-4.84]; P = 0.003). Low-flow alarms rehospitalizations were higher in the LVEDD <55 mm cohort (17.4 vs 8.3%; HR: 2.39 [95% CI: 1.59-3.59]; P < 0.001).

CONCLUSIONS

Although infrequent in occurrence, smaller LVEDD (<55 mm) is associated with increased risk for early and late mortality, a consequence of hemocompatibility-related and right heart failure-related deaths. Rehospitalizations due to low-flow alarms are also more frequent. (MOMENTUM 3 IDE Clinical Study Protocol [HM3™]; NCT02224755; MOMENTUM 3 Continued Access Protocol [MOMENTUM 3 CAP]; NCT02892955).

摘要

背景

先前的分析表明,较小的左心室舒张末期内径(LVEDD)与植入HeartMate 3左心室辅助装置后的生存率降低有关。

目的

在这项基于试验的综合分析中,作者试图研究这一特定关系的临床特征及其与结局的关联。

方法

作者在MOMENTUM 3(使用HeartMate 3进行机械循环支持治疗的患者中磁悬浮技术的多中心研究)试验组合中的1921例可分析的HeartMate 3患者中分析LVEDD<55 mm的情况,以2年时的总生存率和不良事件为终点。不良事件包括血液相容性相关(中风、出血和泵血栓形成)和非血液相容性相关(右心衰竭、感染)结局。

结果

与LVEDD≥55 mm组(n = 1813)相比,LVEDD较小(<55 mm)的患者(n = 108)年龄更大(63±11岁对60±12岁;P = 0.005),女性比例更高(31%对20%;P = 0.096),缺血性心肌病更多(60.2%对42.6%;P = 0.0004)。LVEDD<55 mm组植入住院期间的死亡率更高(14.8%对5.7%;P = 0.0007),2年生存率更低(63.3%对81.8%;HR:1.97 [95%CI:1.39 - 2.79];P = 0.0002)。LVEDD<55 mm组因血液相容性相关不良事件导致的死亡更多(2.8%对0.6%;HR:4.61 [95%CI:1.29 - 16.45];P = 0.018),以及右心衰竭,包括早期(0 - 30天;7.4%对2.0%;HR:3.70 [95%CI:1.73 - 7.91];P = 0.001)和晚期(>30天;12.0%对4.8%;HR:2.58 [95%CI:1.37 - 4.84];P = 0.003)。LVEDD<55 mm队列中因低流量警报再次住院的比例更高(17.4%对8.3%;HR:2.39 [95%CI:1.59 - 3.59];P < 0.001)。

结论

尽管发生率较低,但较小的LVEDD(<55 mm)与早期和晚期死亡风险增加有关,这是血液相容性相关和右心衰竭相关死亡的结果。因低流量警报导致的再次住院也更频繁。(MOMENTUM 3 IDE临床研究方案[HM3™];NCT02224755;MOMENTUM 3持续接入方案[MOMENTUM 3 CAP];NCT02892955)

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